Complex autism spectrum disorder in a patient with a 17q12 microduplication
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Title
Complex autism spectrum disorder in a patient with a 17q12 microduplication
Authors
Keywords
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Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 158A, Issue 5, Pages 1170-1177
Publisher
Wiley
Online
2012-04-05
DOI
10.1002/ajmg.a.35267
References
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Related references
Note: Only part of the references are listed.- Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications
- (2011) Pengfei Liu et al. HUMAN MOLECULAR GENETICS
- Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
- (2010) Daniel Moreno-De-Luca et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome
- (2010) Susanne Ledig et al. FERTILITY AND STERILITY
- Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization
- (2010) Stuart A Scott et al. GENETICS IN MEDICINE
- Autism in three patients with cystic or hyperechogenic kidneys and chromosome 17q12 deletion
- (2010) Chantal Loirat et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study
- (2009) Gian Paolo Ramelli et al. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
- Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12
- (2009) Sandesh Chakravarthy Sreenath Nagamani et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Transcriptional control of axonal guidance and sorting in dorsal interneurons by the Lim-HD proteins Lhx9 and Lhx1
- (2009) Oshri Avraham et al. Neural Development
- Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports
- (2009) Laura Bernardini et al. Orphanet Journal of Rare Diseases
- Structural Variation of Chromosomes in Autism Spectrum Disorder
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a novel microduplication in ASMT
- (2008) Guiqing Cai et al. BMC Medical Genomics
- Private inherited microdeletion/microduplications: Implications in clinical practice
- (2008) Maria Antonietta Mencarelli et al. European Journal of Medical Genetics
- Advances in autism genetics: on the threshold of a new neurobiology
- (2008) Brett S. Abrahams et al. NATURE REVIEWS GENETICS
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
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